The Safety Rates Drug Report

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Drug     Injury     Quarter    

Person who experienced the adverse event (patient)

Event ID CASEID CASEVERSION I F COD EVENT DT MFR DT INIT FDA DT FDA DT REPT COD AUTH NUM MFR NUM MFR SNDR LIT REF AGE AGE COD AGE GRP GNDR COD E SUB WT WT COD REPT DT TO MFR OCCP COD REPORTER COUNTRY OCCR COUNTRY
127106231 12710623 1 I 20160819 20160829 20160902 20160902 PER US-CELGENEUS-USA-2016087634 CELGENE 78.39 YR M Y 70.37000 KG 20160902 MD US US

Drug(s) used by person

Event ID CASEID DRUG SEQ ROLE COD DRUGNAME PROD AI VAL VBM ROUTE DOSE VBM CUM DOSE CHR CUM DOSE UNIT DECHAL RECHAL LOT NUM EXP DT NDA NUM DOSE AMT DOSE UNIT DOSE FORM DOSE FREQ
127106231 12710623 1 PS REVLIMID LENALIDOMIDE 1 Oral N U A2238A 21880 20 MG CAPSULES
127106231 12710623 2 SS REVLIMID LENALIDOMIDE 1 Oral N U A2238A 21880 20 MG CAPSULES
127106231 12710623 3 SS SINEMET CARBIDOPALEVODOPA 1 Unknown U 0 UNKNOWN

Indications of drugs used

Event ID CASEID INDI DRUG SEQ INDI PT
127106231 12710623 1 Plasma cell myeloma
127106231 12710623 3 Parkinson's disease

Outcome of event

Event ID CASEID OUTC COD
127106231 12710623 OT

Reactions reported

Event ID CASEID DRUG REC ACT PT
127106231 12710623 Dizziness
127106231 12710623 Fall

Reporting Sources (this data is often not reported and may therefore be missing here)

no results found

Therapies reported

Event ID CASEID DSG DRUG SEQ START DT END DT DUR DUR COD
127106231 12710623 1 20160805 20160812 0
127106231 12710623 2 20160819 0
127106231 12710623 3 20160805 0